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Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis von McLaughlin, RL, Diekstra, FP, van der Spek, RA, Robinson, MR, Fogh, I, van Doormaal, PT, Tazelaar, GH, Koppers, M, Blokhuis, AM, Sproviero, W, Jones, AR, van Eijk, KR, Harschnitz, O, Vajda, A, Lin, K, Rogelj, B, Vrabec, K, Ravnik-Glavač, M, Koritnik, B, Zidar, J, Leonardis, L, Millecamps, S, de Carvalho, M, Mora, JS, Rojas-García, R, Polak, M, Chandran, S, Swingler, R, Morrison, KE, Shaw, PJ, Hardy, J, Orrell, RW, Malaspina, A, Abdulla, S, Sendtner, M, Ophoff, RA, Staats, KA, Trojanowski, JQ, Elman, L, McCluskey, L, Hamzeiy, H, Meitinger, T, Radivojkov-Blagojevic, M, Andres, CR, Maurel, C, Brice, A, Dürr, A, Tittmann, L, Franke, A, Amouyel, P, Dartigues, JF, Rivadeneira, F, Hofman, A, van der Kooi, AJ, Pansarasa, O, Cereda, C, Del Bo, R, Comi, GP, Sorarù, G, Mazzini, L, Gellera, C, Ratti, A, Calvo, A, Brunetti, M, Arcuti, S, Capozzo, R, Zecca, C, Penco, S, Riva, N, Filosto, M, Muller, B, PARALS Registry, SLAP Registry, SLAGEN Consortium, NNIPPS Study Group, Blair, I, Zhang, K, Nicholson, GA, Rowe, DB, Pamphlett, R, Grosskreutz, J, Prell, T, Casale, F, Chio, A, Beghi, E, Pupillo, E, Weishaupt, JH, Pers, TH, Brown, RH, Hardiman, O, Andersen, PM, Corcia, P, Vourc'h, P, Wray, NR, de Bakker, PI, van Es, MA, Pasterkamp, RJ, Lewis, CM, Breen, G, van den Berg, LH

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